(57) A compound of the formula (I):
 wherein
W, and W2 each independently is a hydrogen atom or a
 group wherein Y is a n-C1-6 alkvlene group or a n-C1-6 alkylene group having a C1-6 alkyl group substituent; and R, and R2 each independently is a hydrogen atom or a C1-5 alkyl group, and
 group in
 group may form a saturated heterocyclic ring selected from the group consisting of
morphohno. pyrrolidino, piperidino, homopiperidino and piperazino groups. and the
saturated heterocyclic ring except the morpholino group may have at least one C1-4 alkyl group, hydroxyl group or halogen atom as a substituent;
Z, is a hydrogen atom, a chlorine atom, a bromine atom, an iodine atom, a hydroxyl
group, an amino group, a C1-3 alkyl group or a methoxy group;
Z2 is a hydrogen atom or an amino group;
when W, and W2 are both hydrogen atoms, Z, is a hydroxyl group or an iodine atom and Z2 is hydrogen atom, or Z, and 22 are both amino groups;
When Z, and 22 are both hydrogen atoms, the
 group in either W, or W2 is a morpholino group;
when Z, is a chlorine atom, a hydroxyl group, an iodine atom, a methyl group or a
methoxy group, Z2 is a hydrogen atom;
when Z, is an amino group, Z2 is a hydrogen atom or an amino group;
when Z, is a methyl group, a methoxy group or an amino group, Z, is in the 5-position;
when Z, is an iodine atom, Z, is in the 5- or 7-position; and when Z, and Z2 are both amino groups. Z, and Z2 are in the 5- and 7-positions; and the physiologically acceptable acid addition salt
thereof.
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